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一种光激活的 Ru(II)配合物,带有 2,9-二苯基-1,10-菲啰啉:一种有效的化疗药物,能诱导三阴性人乳腺癌腺癌细胞凋亡。

A photoactivatable Ru (II) complex bearing 2,9-diphenyl-1,10-phenanthroline: A potent chemotherapeutic drug inducing apoptosis in triple negative human breast adenocarcinoma cells.

机构信息

Faculty of Health and Medical Sciences, Department of Microbial and Cellular Sciences, University of Surrey, UK; Department of Natural Sciences, Lebanese American University, Chouran, Beirut, 1102-2801, Lebanon.

Faculty of Health and Medical Sciences, Department of Microbial and Cellular Sciences, University of Surrey, UK.

出版信息

Chem Biol Interact. 2021 Feb 25;336:109317. doi: 10.1016/j.cbi.2020.109317. Epub 2020 Nov 13.

Abstract

The photoactivatable Ru (II) complex 1 [Ru(bipy)2(dpphen)]Cl2 (where bipy = 2,2'-bipyridine and dpphen = 2,9-diphenyl-1,10-phenanthroline) has been shown to possess promising anticancer activity against triple negative adenocarcinoma MDA-MB-231 cells. The present study aims to elucidate the plausible mechanism of action of the photoactivatable complex 1 against MDA-MB-231 cells. Upon photoactivation, complex 1 exhibited time-dependent cytotoxic activity with a phototoxicity index (P Index) of >100 after 72 h. A significant increase in cell rounding and detachment, loss of membrane integrity, ROS accumulation and DNA damage was observed. Flow cytometry and a fluorescent apoptosis/necrosis assay showed an induction of cell apoptosis. Western blot analysis revealed the induction of intrinsic and extrinsic pathways and inhibition of the MAPK and PI3K pathways. The photoproduct of complex 1 showed similar effects on key apoptotic protein expression confirming that it is behind the observed cell death. In conclusion, the present study revealed that complex 1 is a potent multi-mechanistic photoactivatable chemotherapeutic drug that may serve as a potential lead molecule for targeted cancer chemotherapy.

摘要

光激活型钌(II)配合物 1 [Ru(bipy)2(dpphen)]Cl2(其中 bipy=2,2'-联吡啶,dpphen=2,9-二苯基-1,10-菲咯啉)已被证明对三阴性腺癌 MDA-MB-231 细胞具有有前景的抗癌活性。本研究旨在阐明光激活型配合物 1 对 MDA-MB-231 细胞的可能作用机制。光激活后,配合物 1 在 72 小时后表现出时间依赖性细胞毒性活性,光毒性指数(P 指数)>100。观察到细胞圆化和脱落、膜完整性丧失、ROS 积累和 DNA 损伤显著增加。流式细胞术和荧光细胞凋亡/坏死检测显示细胞凋亡的诱导。Western blot 分析显示诱导了内在和外在途径,并抑制了 MAPK 和 PI3K 途径。配合物 1 的光产物对关键凋亡蛋白表达显示出相似的影响,证实了观察到的细胞死亡是由其引起的。总之,本研究表明,配合物 1 是一种有效的多机制光激活化疗药物,可能成为靶向癌症化疗的潜在先导分子。

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